College of Engineering, Mathematics and Physical Sciences, University of Exeter, Exeter, EX4 4QF, United Kingdom.
State Key Laboratory of Chemical Resource Engineering, Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P.R. China.
Sci Rep. 2017 Jul 13;7(1):5266. doi: 10.1038/s41598-017-05636-y.
A series of nanocomposites of cobalt embedded in N-doped nanoporous carbons, carbon nanotubes or hollow carbon onions have been synthesized by a one-step carbonization of metal-organic-framework ZIF-67. The effect of the carbonization temperature on the structural evolution of the resulting nanocomposites has been investigated in detail. Among the as-synthesized materials, the cobalt/nanoporous N-doped carbon composites have demonstrated excellent electrocatalytic activities and durability towards oxygen reduction reaction in alkaline medium. Compared to the benchmark Pt/C catalyst, the optimized Co@C-800 (carbonized at 800 °C) exhibited high oxygen reduction reaction activity with an onset potential of 0.92 V, and a half-wave potential of 0.82 V. Moreover, the optimized Co@C-800 also showed enhanced electrocatalytic activity towards oxygen evolution reaction from water splitting, with a low onset potential of 1.43 V and a potential of 1.61 V at 10 mA cm current density. This work offered a simple solution to develop metal-organic-framework-derived materials for highly efficient electrochemical applications.
一系列钴嵌入氮掺杂纳米多孔碳、碳纳米管或空心碳洋葱的纳米复合材料已通过金属有机骨架 ZIF-67 的一步碳化合成。详细研究了碳化温度对所得纳米复合材料结构演化的影响。在所合成的材料中,钴/纳米多孔氮掺杂碳复合材料在碱性介质中对氧还原反应表现出优异的电催化活性和耐久性。与基准 Pt/C 催化剂相比,优化后的 Co@C-800(在 800°C 碳化)具有高的氧还原反应活性,起始电位为 0.92 V,半波电位为 0.82 V。此外,优化后的 Co@C-800 对水分解的析氧反应也表现出增强的电催化活性,起始电位低至 1.43 V,在 10 mA·cm-2电流密度时的电位为 1.61 V。这项工作为开发用于高效电化学应用的金属有机骨架衍生材料提供了一种简单的解决方案。